A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1320n223



Internal ID22804288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116796501..116802972hg38UCSC Ensembl
chr11:116667217..116673688hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386472
hg196472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6466803, nsv6459644, nsv6468390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1320n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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